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MC2X Two-Stage Venous Cannula - SFDA Registration ME0000000256SFDAA00762

Access comprehensive regulatory information for MC2X Two-Stage Venous Cannula in the Saudi Arabia medical device market through Pure Global AI's free database. This Class III device is registered with Saudi Arabia SFDA under registration number ME0000000256SFDAA00762 and manufactured by Medtronic, Inc..

This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.

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Class III
ME0000000256SFDAA00762
MC2X Two-Stage Venous Cannula
SFDA Registration: ME0000000256SFDAA00762
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Product Information

Coated Venous Cannula

Product Use

This cannula is intended for use in venous drainage via the right atrium and inferior vena cava simultaneously during cardiopulmonary bypass surgery for up to 6 hours.

Device Classification
Risk Class
Class III
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000000256SFDAA00762
Authorization ID
GHTF-2018-1835
Status
Active
Expire Date
September 15, 2023
Manufacturer
Manufacturer Name
Medtronic, Inc.
Model Information
Model ID(s)
CB91429; CB91429C; CB91437C;
Product Accessories

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